Pilot Trial Investigating Every Other Day Dosing of Oral Iron in Premature Infants (IQONic)
Recruiting
N/A
Interventional Study
Very Low Birth Weight Infant
Premature Infants
Anemia of Prematurity
Iron Deficiency, Anaemia in Children
Extremely Low Birth Weight
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 26 Weeks – 32 Weeks
- Sex
- Any
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 100 (estimated)
- Sponsor
- CHRISTUS Health · Other
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About This Trial
Study focuses on determining if daily versus every-other-day (EOD) oral iron at the same dose per kilogram per day will achieve similar incidence of iron replete status at 36 weeks post-menstrual age in premature neonates
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Children (Minor \< 18 years of age)
* Neonates
* Hospitalized
* Premature infants who are on full enteral feeds and are started on oral iron
* Premature infants who completed 26 0/7 to 32 6/7 weeks' gestation at birth
Exclusion Criteria:
• Infants with known congenital anoma…
Contacts